Senior CRA (Oncology)

Piper Companies; United States; Remote; USD 83,000 - 110,000; Full time

Benefits offered by this job

Travel reimbursement

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (Oncology) for a fully remote contract position in the United States, with regional travel to trial sites. The role suits an experienced CRA with a strong oncology background, independent monitoring skills, and the ability to manage multiple sites with minimal oversight.

Responsibilities include site monitoring, guidance to investigative sites, and oversight of data quality, patient safety, and site performance across study phases.

Qualifications

• Independent monitoring experience required.
• Full clinical trial lifecycle management experience.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience with oncology trials and protocols.
• Willingness to travel 25–40%.

Responsibilities

• Perform site monitoring visits across study phases while ensuring protocol, regulatory, and GCP compliance.
• Maintain direct communication with investigative sites, guiding and resolving study-related challenges.
• Oversee oncology study activities by reviewing data quality, patient safety, and site performance.
• Manage multiple trial sites simultaneously, prioritizing deliverables and tracking milestones.
• Collaborate with biotech sponsors and internal teams to support timely trial execution.

Skills

Independent monitoring

Clinical trial lifecycle

ICH-GCP knowledge

FDA regulations

Oncology protocols

Travel readiness

Job description

Piper Companies is seeking a Senior Clinical Research Associate (Oncology) to support a client in the biotechnology industry in the United States. The Senior Clinical Research Associate (Oncology) role is a fully remote contract position with regional travel required to clinical trial sites. The Senior Clinical Research Associate (Oncology) role is ideal for an experienced professional with a strong background in oncology trials, independent monitoring, and managing multiple sites with minimal oversight.

Responsibilities of the Senior Clinical Research Associate (Oncology) include:

• Perform site monitoring visits across study phases, ensuring compliance with protocol, regulatory requirements, and GCP standards
• Maintain direct communication with investigative sites, providing guidance and resolving study-related challenges
• Oversee oncology study activities by reviewing data quality, patient safety measures, and overall site performance
• Manage multiple trial sites simultaneously, prioritizing deliverables and tracking key study milestones
• Collaborate with biotech sponsors and internal teams to support efficient and timely trial execution

Requirements of the Senior Clinical Research Associate (Oncology) include:

• 5+ years of CRA experience with at least 2+ years supporting oncology clinical trials
• Strong experience with independent monitoring and full clinical trial lifecycle management
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and oncology protocols
• Experience working directly with biotech or sponsor clients in a fast-paced environment
• Ability to manage multiple priorities effectively with approximately 25-40% travel

Compensation for the Senior Clinical Research Associate (Oncology) include:

• $60 – $80/hour
• Contract role
• Travel reimbursement provided

This job opens for applications on 9/18/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Senior Clinical Research Associate, CRA, Oncology, Clinical Trials, Remote, Contract, Monitoring, Biotech

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